量化基于 X 射线计算机断层扫描的生物标志物以评估髋部骨折风险的分割方法:系统性文献综述。

IF 4.3 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Frontiers in Bioengineering and Biotechnology Pub Date : 2024-10-23 eCollection Date: 2024-01-01 DOI:10.3389/fbioe.2024.1446829
Cristina Falcinelli, Vee San Cheong, Lotta Maria Ellingsen, Benedikt Helgason
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引用次数: 0

摘要

背景:使用骨矿物质密度和/或 FRAX 预测股骨骨质疏松性骨折风险的成功率并不高,因为它们没有考虑到影响骨折风险的机械决定因素。目前已开发出基于计算机断层扫描(CT)的几何、密度和有限元衍生生物标志物,并将其用作评估骨折风险的参数。然而,要量化这些生物标志物,需要对 CT 数据进行分割。手动或半自动完成这项工作耗费大量人力物力,阻碍了这些生物标志物在临床实践中的应用。近年来,全自动 CT 数据分割方法开始出现。量化这些分割工具的准确性、稳健性、再现性和可重复性对于研究和将基于 CT 的生物标记物转化为临床实践具有重要意义:方法:在 PubMed 上对截至 2024 年 7 月底的文献进行了全面检索。只有在人体股骨和/或骨盆以及临床和非临床 CT 上经过定量验证的分割方法才被纳入。对这些分割方法的准确性、稳健性、再现性和可重复性进行了研究,并定量报告了用于评估这些方面的分割指标。对纳入的研究进行了评估,以确定可能影响报告结果的偏倚风险和来源:共有 54 项研究符合纳入标准。对所纳入论文的分析表明,自动分割方法可得出准确的结果,但可能需要对不同研究的准确性报告进行标准化。很少有研究对稳健性进行调查,因此无法就此得出详细结论。最后,骨分割领域似乎只在非常有限的程度上探讨了可重复性和可重复性的概念,这就意味着大多数研究都存在很高的偏倚风险:根据所分析的研究,我们为未来的研究提出了一些建议,以推动标准化分割方案的发展。此外,还提出了评估分割方法准确性、稳健性、再现性和可重复性的标准化指标,以方便对不同方法进行比较。
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Segmentation methods for quantifying X-ray Computed Tomography based biomarkers to assess hip fracture risk: a systematic literature review.

Background: The success of using bone mineral density and/or FRAX to predict femoral osteoporotic fracture risk is modest since they do not account for mechanical determinants that affect bone fracture risk. Computed Tomography (CT)-based geometric, densitometric, and finite element-derived biomarkers have been developed and used as parameters for assessing fracture risk. However, to quantify these biomarkers, segmentation of CT data is needed. Doing this manually or semi-automatically is labor-intensive, preventing the adoption of these biomarkers into clinical practice. In recent years, fully automated methods for segmenting CT data have started to emerge. Quantifying the accuracy, robustness, reproducibility, and repeatability of these segmentation tools is of major importance for research and the potential translation of CT-based biomarkers into clinical practice.

Methods: A comprehensive literature search was performed in PubMed up to the end of July 2024. Only segmentation methods that were quantitatively validated on human femurs and/or pelvises and on both clinical and non-clinical CT were included. The accuracy, robustness, reproducibility, and repeatability of these segmentation methods were investigated, reporting quantitatively the metrics used to evaluate these aspects of segmentation. The studies included were evaluated for the risk of, and sources of bias, that may affect the results reported.

Findings: A total of 54 studies fulfilled the inclusion criteria. The analysis of the included papers showed that automatic segmentation methods led to accurate results, however, there may exist a need to standardize reporting of accuracy across studies. Few works investigated robustness to allow for detailed conclusions on this aspect. Finally, it seems that the bone segmentation field has only addressed the concept of reproducibility and repeatability to a very limited extent, which entails that most of the studies are at high risk of bias.

Interpretation: Based on the studies analyzed, some recommendations for future studies are made for advancing the development of a standardized segmentation protocol. Moreover, standardized metrics are proposed to evaluate accuracy, robustness, reproducibility, and repeatability of segmentation methods, to ease comparison between different approaches.

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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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